Cytyc Surgical Products

Abbott Laboratories Corporation

Cytyc Corporation

Novacept, Inc.

Stephanie R Squarcia

Russel Mahlon Sampson

Estela Hilario

Csaba Truckai

Alfonso Lawrence Ramirez

Andrew J Scherer

Michael W Lawless

Peter A Soberon

Alfonzo Lawrence Ramirez

David C Auth

John D Gjata

An apparatus and method for use in performing ablation or coagulation of organs and other tissue includes a metallized fabric electrode array which is substantially absorbent and/or permeable to moisture and gases such as steam and conformable to the body cavity. Following placement of the ablation device into contact with the tissue to be ablated, an RF generator is used to deliver RF energy to the conductive regions and to thereby induce current flow from the electrodes to tissue to be ablated. As the current heats the tissue, moisture (such as steam or liquid) leaves the tissue causing the tissue to dehydrate. Suction may be applied to facilitate moisture removal. The moisture permeability and/or absorbency of the electrode carrying member allows the moisture to leave the ablation site so as to prevent the moisture from providing a path of conductivity for the current.

Moisture transport system for contact electrocoagulation

An apparatus and method for use in performing ablation or coagulation of organs and other tissue includes a metallized fabric electrode array which is substantially absorbent and/or permeable to moisture and gases such as steam and conformable to the body cavity. The array includes conductive regions separated by insulated regions arranged to produce ablation to a predetermined depth. Following placement of the ablation device into contact with the tissue to be ablated, an RF generator is used to deliver RF energy to the conductive regions and to thereby induce current flow from the electrodes to tissue to be ablated. As the current heats the tissue, moisture (such as steam or liquid) leaves the tissue causing the tissue to dehydrate. Suction may be applied to facilitate moisture removal. The moisture permeability and/or absorbency of the electrode carrying member allows the moisture to leave the ablation site so as to prevent the moisture from providing a path of conductivity for the current.

An apparatus and method for use in performing ablation or coagulation of organs and other tissue includes a metallized fabric electrode array which is substantially absorbent and/or permeable to moisture and gases such as steam and conformable to the body cavity. The array includes conductive regions separated by insulated regions arranged to produce ablation to a predetermined depth. Following placement of the ablation device into contact with the tissue to be ablated, in RF generator is used to deliver RF energy to the conductive regions and to thereby induce current flow from the electrodes to tissue to be ablated. As the current heats the tissue, moisture (such as steam or liquid) leaves the tissue causing the tissue to dehydrate. Suction may be applied to facilitate moisture removal. The moisture permeability and/or absorbency of the electrode carrying member allows the moisture to leave the ablation site so as to prevent the moisture from providing a path of conductivity for the current.

Method for ablating and/or coagulating tissue using moisture transport

A drive connector for elastomerically coupling a drive shaft to a driven shaft. An elastomeric coupling includes openings on opposite ends that are generally &ldquo;D&rdquo;-shaped forming an interference fit with correspondingly shaped ends of the drive shaft and the driven shaft. A web extends transversely within the interior of the elastomeric coupling, limiting the distance that the drive shaft and driven shaft are inserted within the openings of the coupling. The coupling includes a rib that runs longitudinally along its outer length. A sleeve having a groove corresponding in size and shape to the rib is slipped over the coupling and is connected to the driven shaft. The sleeve includes a rigid interior element that is overmolded with an elastomeric material. A cam bearing is fitted over a cam surface on the sleeve and provides a force in one direction, urging a plunger to displace an elastomeric membrane in a pumping cassette, forcing medicinal fluid to flow through the pumping cassette. The elastomeric membrane provides the restoring force to the plunger, so that a loop formed on the upper portion of the plunger and disposed around the cam bearing does not receive any force from the cam bearing to move the plunger away from the pump cassette. The elastomeric coupling and sleeve form a relatively compact assembly for coupling the drive shaft to the driven shaft and accommodate minor misalignment between the center lines of the drive shaft and the driven shaft.

Elastomeric connector coupling motor to cam actuator of infusion pump

In a pump chassis (,), spring-loaded members (,) engage a pumping cassette (,) to it in a predetermined position. The members each include pairs of latches (110,, 110,) that are each beveled to form a ramp so that the latches and associated members are forced outwardly to enable the pumping cassette to be seated within the pump chassis. The latches engage the pump cassette as it is seated, holding it securely. A release button (,) is attached to a spring-loaded shaft (,) that extends into the interior of the pump chassis. The shaft has a ramp formed on its inner end. When the user depresses the release button, the ramp rides under inwardly extending arms (,) provided on the members, forcing the members and attached latches to move outwardly. As the members move outwardly, the pumping cassette is released and readily removed.

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Palo Alto, CA, United States of America

Stephanie R Squarcia